8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LE-12CH
FDA 510(k)
FDA Class 2
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517629685·CoRoent Ant TLIF Ti, 12x10x36mm 12°
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996134170·LATERAL,CURETTE,STRAIGHT CUP
METAFIX FEMORAL STEM FOR HEMI-ARTHROPLASTY
FDA 510(k)
FDA Class 2
·Orthopedic
P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
ADULT BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·October 31, 2008
NC QUANTUM APEX PTCA DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·August 23, 2011
QUADRA ASSURA CRT-D, DF4 CONNECTOR
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·July 11, 2013